LL Mini Onebody Implant
The LL Mini Onebody Implant replaces missing mandibular central or lateral incisors in partially edentulous patients. It supports dental prosthetic devices to restore chewing function and…
The LL Mini Onebody Implant replaces missing mandibular central or lateral incisors in partially edentulous patients. It supports dental prosthetic devices to restore chewing function and is intended for delayed loading. The implant is designed for a single use.
The one-piece implant is made from commercially pure Grade 4 titanium. It has a tapered threaded body with a cutting edge and a sandblasted, acid-etched surface. The implant is placed in bone as the support for the dental restoration.
Listed Item
Dental Implant Fixture
Supply and Protection
The implant is supplied sterile after gamma irradiation. A separate temporary cap protects its upper portion in the mouth; that cap is supplied nonsterile and requires sterilization before use.
Who Else Makes It
Concentrated in Jiangsu (3), Sichuan (2), Shanghai (1). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Changzhou Biomet Medical Devices Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 54 |
| LX Precision Shanghai Co Ltd | Shanghai | Shanghai | Contract manufacturer | 19 |
| Jiangsu Trausim Medical Instrument Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 3 |
| Basic (Chengdu) Medical Device Co., Ltd. | Chengdu | Sichuan | Contract manufacturer | 1 |
| Dongguan Xinlonghong Hardware Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 1 |
| Chengdu Besmile Medical Technology Co., Ltd. | Chengdu | Sichuan | Manufacturer | 14 |
| BIO Concept Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 5 |
Record
| Listed by | Ossvis Co., Ltd., South Korea |
|---|---|
| FDA product code | DZE |
| Device type | Implant, Endosseous, Root-Form |
| Device class | Class 2 |
| Regulation | 21 CFR 872.3640 |
| Establishment | Manufacturer |
| 510(k) | K242379 |
| Record published | 2024-11-29 |
| Record revised | 2025-07-02 (version 2) |
Specifications
| MRI safety | MR Conditional |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| LLMF251140S | In distribution | |
| LLMF301040S | In distribution | |
| LLMF251040S | In distribution | |
| LLMF251340S | In distribution | |
| LLMF251335S | In distribution | |
| LLMF250820S | In distribution | |
| LLMF301130S | In distribution | |
| LLMF301330S | In distribution | |
| LLMF300830S | In distribution | |
| LLMF301340S | In distribution | |
| LLMF301020S | In distribution | |
| LLMF301125S | In distribution | |
| LLMF251320S | In distribution | |
| LLMF251030S | In distribution | |
| LLMF251120S | In distribution | |
| LLMF250835S | In distribution | |
| LLMF250840S | In distribution | |
| LLMF301140S | In distribution | |
| LLMF250830S | In distribution | |
| LLMF300835S | In distribution | |
| LLMF301325S | In distribution | |
| LLMF251035S | In distribution | |
| LLMF300820S | In distribution | |
| LLMF301025S | In distribution | |
| LLMF301030S | In distribution | |
| LLMF300840S | In distribution | |
| LLMF301540S | In distribution | |
| LLMF301320S | In distribution | |
| LLMF251135S | In distribution | |
| LLMF251025S | In distribution | |
| LLMF251020S | In distribution | |
| LLMF251330S | In distribution | |
| LLMF251325S | In distribution | |
| LLMF301120S | In distribution | |
| LLMF301035S | In distribution | |
| LLMF300825S | In distribution | |
| LLMF250825S | In distribution | |
| LLMF301135S | In distribution | |
| LLMF251130S | In distribution | |
| LLMF251125S | In distribution | |
| LLMF301335S | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Neodent | Jjgc Indústria e Comércio de Materiais Dentários S.A. | 920 |
| Osstem Implant System | Osstem Implant Co., Ltd. | 788 |
| Magicore | InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) | 744 |
| Implant, Endosseous, Root-Form | Southern Implants (PTY) Ltd | 608 |
| ITL Dental | Emery Enterprises Inc. | 603 |
| Magicore S | InnoBioSurg Co., Ltd.(IBS implant Co., Ltd.) | 560 |
| Friadent® | Dentsply Implants Manufacturing GmbH | 525 |
| Sphero Block Normo | Rhein 83 SRL | 489 |
| Neobiotech Implant System | Neobiotech Co., Ltd. | 483 |
| KJ Mini Implant System | Kjmeditech.co., Ltd. | 448 |
| Ritter Dental Implant System | Ritter Implants GmbH & Co. KG | 418 |
| Leone SPA | Leone SPA | 404 |
Showing 12 of 2,762. All products under Implant, Endosseous, Root-Form
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K242379 | 2024-11-07 |
| K233808 | 2024-07-31 |
| K223924 | 2023-08-08 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P800035 | 2001-10-04 | PERI-OSS | Curasan AG |
| P860012 | 1988-10-28 | ALVEOFORM TM BIOGRAFT | Collagen Corp. |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.